Site Contracts Template Specialist

hace 1 semana

Madrid, Madrid, España Pfizer A tiempo completo

Job Summary

The Site Contracts Template Specialist is a critical role within Pfizer's Clinical Development team, responsible for identifying and prioritizing opportunities to maintain and improve site contract templates. This position requires a strong understanding of the biopharmaceutical industry and the ability to draft, review, and communicate changes to site contract templates.

Key Responsibilities

  • Develop and maintain a deep understanding of Pfizer's clinical development operations and the biopharmaceutical industry.
  • Identify and prioritize opportunities to improve site contract templates, ensuring alignment with changing external and internal requirements.
  • Draft, review, and communicate changes to site contract templates, collaborating with Pfizer Legal to ensure compliance.
  • Manage the introduction of revised templates, gaining approvals and communicating changes to stakeholders.
  • Update contract template guidance and repository to support contract template changes.
  • Ensure training is delivered and documented to site contracting professionals on Investigative Site Contracting policies, templates, and standards.
  • Negotiate or oversee the negotiation and execution of assigned contracts.

Requirements

  • 7+ years of experience in clinical development operations or clinical trial outsourcing, with a bachelor's degree or equivalent.
  • Experience working with limited supervision to achieve business goals.
  • Strong understanding of contracts and negotiation principles, practices, processes, and activities.
  • Balance of general business, compliance, finance, legal, and drug development or legal/compliance experience in a regulated industry.
  • Strong and precise communications and presentation skills.
  • Record of achievement and delivery against personal goals.
  • Demonstrated ability to lead by influence rather than positional power to accomplish critical deliverables.
  • Demonstrated success in working in a highly matrix-based organization.

Preferred Qualifications

  • 5+ years of experience in clinical development operations or clinical trial outsourcing with a master's degree.
  • 2+ years of experience in clinical development operations or clinical trial outsourcing with a Juris Doctorate (or equivalent).
  • Expertise in drafting and negotiating Clinical Trial Agreements with clinical trial sites in a global operation.

Benefits

Pfizer offers a comprehensive and generous benefits package, including a 401(k) plan, paid vacation, holiday, and personal days, paid caregiver/parental and medical leave, and health benefits.

Equal Opportunity Employer

Pfizer is an equal opportunity employer and complies with all applicable national, state, and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.

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